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Table 2 Single-marker analysis between SNPs and categorical DD.

From: Association of the rs3743205 variant of DYX1C1 with dyslexia in Chinese children

rs Number

SNP

Position

Location

Allele

F

OR (95% CI)

Nominal p-value

FDR q-value

rs8040756

A/G

26589156

Intron 1

A*

0.135

1.43 (0.88 - 2.32)

0.1445

0.2823

    

G

0.865

   

rs3743205

G/A

26581087

5' UTR

G*

0.982

0.08 (0.01 - 0.64)

0.0009

0.0072

    

A

0.018

   

rs4255730

C/T

26578338

Intron 3

C*

0.670

0.85 (0.59 - 1.23)

0.3969

0.6202

    

T

0.330

   

rs692646

A/G

26557344

Intron 4

A*

0.067

2.00 (0.96 - 4.12)

0.0532

0.1385

    

G

0.933

   

rs692691

C/T

26551132

Intron 4

C*

0.947

0.86 (0.40 - 1.85)

0.6947

0.8455

    

T

0.053

   

rs2290981

A/G

26550245

Intron 4

A*

0.119

1.10 (0.60 - 2.02)

0.7575

0.8455

    

G

0.881

   

rs4774768

G/T

26517062

Intron 8

G*

0.189

1.68 (1.02 - 2.76)

0.0367

0.1385

    

T

0.811

   

rs57809907

G/T

26513439

Exon 10

T*

0.004

1.00 (0.06 - 15.99)

1.0000

0.9766

    

G

0.996

   
  1. F = Allele frequency
  2. *Reference allele